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1
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0028880055
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For example, Nicolau's landmark synthesis ot brevetoxin B: Nicolau, K. C.; Theodorakis, E. A.; Rutjes, F. P. J. T.; Tiebes, J.; Sato, M.; Untersteller, E.; Xiao, X.-Y. J. Am. Chem. Soc. 1995, 117, 1171-1172.
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For example, Nicolau's landmark synthesis ot brevetoxin B: Nicolau, K. C.; Theodorakis, E. A.; Rutjes, F. P. J. T.; Tiebes, J.; Sato, M.; Untersteller, E.; Xiao, X.-Y. J. Am. Chem. Soc. 1995, 117, 1171-1172.
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2
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0028806793
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Nicolau, K. C.; Rutjes, F. P. J. T.; Theodorakis, E. A.; Tiebes, J.; Sato, M.; Untersteller, E. J. Am. Chem. Soc. 1995, 117, 1173-1174.
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(1995)
J. Am. Chem. Soc
, vol.117
, pp. 1173-1174
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Nicolau, K.C.1
Rutjes, F.P.J.T.2
Theodorakis, E.A.3
Tiebes, J.4
Sato, M.5
Untersteller, E.6
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3
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0010057116
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For an intriguing personalized account of these efforts see
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For an intriguing personalized account of these efforts see: Nicolau, K. C. Angew. Chem., Int. Ed. Engl. 1996, 35, 589-607.
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(1996)
Angew. Chem., Int. Ed. Engl
, vol.35
, pp. 589-607
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Nicolau, K.C.1
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4
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0000563379
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(a) Alvarez, E.; Candenas, M. L.; Peréz, R.; Ravelo, J. L.; Martin, J. D. Chem. Rev. 1995, 95, 1953-1980.
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(1995)
Chem. Rev
, vol.95
, pp. 1953-1980
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Alvarez, E.1
Candenas, M.L.2
Peréz, R.3
Ravelo, J.L.4
Martin, J.D.5
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7
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2342522136
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One such example with potential for broader application features ringclosing metathesis in carbohydrate-derived systems: (a) Leeuwenburgh, M. A, Overkleeft, H. S, van der Marel, G. A, van Boom, J. H. Synlett 1997, 1263-1264
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One such example with potential for broader application features ringclosing metathesis in carbohydrate-derived systems: (a) Leeuwenburgh, M. A.; Overkleeft, H. S.; van der Marel, G. A.; van Boom, J. H. Synlett 1997, 1263-1264.
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8
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0033516601
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(b) Leeuwenburgh, M. A.; Kulker, C.; Duynstee, H. I.; Overkleeft, H. S.; van der Marel, G. A.; van Boom, J. H. Tetrahedron 1999, 55, 8253-8262.
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(1999)
Tetrahedron
, vol.55
, pp. 8253-8262
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Leeuwenburgh, M.A.1
Kulker, C.2
Duynstee, H.I.3
Overkleeft, H.S.4
van der Marel, G.A.5
van Boom, J.H.6
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9
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0242385411
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Acid chlorides: Burke, S. D.; Murtiashaw, C. W.; Dike, M. S.; Smith Strickland, S. M.; Saunders, J. O. J. Org. Chem. 1981, 46, 2400-2402.
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Acid chlorides: Burke, S. D.; Murtiashaw, C. W.; Dike, M. S.; Smith Strickland, S. M.; Saunders, J. O. J. Org. Chem. 1981, 46, 2400-2402.
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10
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37049098483
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Nakamura, E.; Fukuzaki, K.; Kuwajima, I. J. Chem. Soc., Chem. Commun. 1983, 499-501.
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(1983)
J. Chem. Soc., Chem. Commun
, pp. 499-501
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Nakamura, E.1
Fukuzaki, K.2
Kuwajima, I.3
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11
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34548528809
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Mikami, K.; Kishi, N.; Nakai, T. Tetrahedron Lett. 1983, 24, 795-798.
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(1983)
Tetrahedron Lett
, vol.24
, pp. 795-798
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Mikami, K.1
Kishi, N.2
Nakai, T.3
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13
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0010364902
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Fukuzaki, K.; Nakamura, E.; Kuwajima, I. Tetrahedron Lett. 1984, 25, 3591-3594.
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(1984)
Tetrahedron Lett
, vol.25
, pp. 3591-3594
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Fukuzaki, K.1
Nakamura, E.2
Kuwajima, I.3
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14
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0025744177
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Aldehydes: McIntosh, M. C.; Weinreb, S. M. J. Org. Chem. 1991, 56, 5010-5012.
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Aldehydes: McIntosh, M. C.; Weinreb, S. M. J. Org. Chem. 1991, 56, 5010-5012.
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16
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84984156755
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Ketones: Hoflack, J.; De Clercq, P. J. Bull. Soc. Chim. Belg. 1983, 92, 407-408.
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Ketones: Hoflack, J.; De Clercq, P. J. Bull. Soc. Chim. Belg. 1983, 92, 407-408.
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17
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0000551884
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Thioacetals: Trost, B. M.; Murayama, E. J. Am. Chem. Soc. 1981, 103, 6529-6530.
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Thioacetals: Trost, B. M.; Murayama, E. J. Am. Chem. Soc. 1981, 103, 6529-6530.
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18
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0000317621
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Overman, L. E.; Casteñada, A.; Blumenkopf, T. A. J. Am. Chem. Soc. 1986, 108, 1303-1304.
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(1986)
J. Am. Chem. Soc
, vol.108
, pp. 1303-1304
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Overman, L.E.1
Casteñada, A.2
Blumenkopf, T.A.3
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19
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33845374627
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However, these latter studies have not always involved full participation of the silyl moiety, having invoked an alternative polar ene mechanism
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Overman, L. E.; Blumenkopf, T. A.; Casteñada, A.; Thompson, A. S. J. Am. Chem. Soc. 1986, 108, 3516-3517. However, these latter studies have not always involved full participation of the silyl moiety, having invoked an alternative polar ene mechanism.
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(1986)
J. Am. Chem. Soc
, vol.108
, pp. 3516-3517
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Overman, L.E.1
Blumenkopf, T.A.2
Casteñada, A.3
Thompson, A.S.4
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20
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0346195421
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A recent analogous approach to bridged oxabicyclics, employing both silicon- and sulfur-activated olefins, proceeded via ene and Prins pathways, respectively: Sasmal, P. K.; Maier, M. E. Org. Lett. 2002, 4, 1271-1274.
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A recent analogous approach to bridged oxabicyclics, employing both silicon- and sulfur-activated olefins, proceeded via ene and Prins pathways, respectively: Sasmal, P. K.; Maier, M. E. Org. Lett. 2002, 4, 1271-1274.
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21
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33845373996
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By contrast the related reaction of iminium ions is a well-established strategy for alkaloid synthesis: Blumenkopf, T, Overman, L. E. Chem. Rev. 1986, 86, 857-873
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By contrast the related reaction of iminium ions is a well-established strategy for alkaloid synthesis: Blumenkopf, T.; Overman, L. E. Chem. Rev. 1986, 86, 857-873.
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23
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0005837446
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This possibility has not been overlooked, as elegantly exploited by Tius in a novel benzene annulation process: Tius, M. A. Tetrahedron Lett. 1981, 22, 3335-3338
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This possibility has not been overlooked, as elegantly exploited by Tius in a novel benzene annulation process: Tius, M. A. Tetrahedron Lett. 1981, 22, 3335-3338.
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26
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0000721788
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In one rate study, an E-vinylsilane reacted >7000 times faster than its corresponding Z-counterpart: Overman, L. E, Burk, R. M. Tetrahedron Lett. 1984, 25, 5739-5742. A similar observation was noted by Fleming, see ref 7
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In one rate study, an E-vinylsilane reacted >7000 times faster than its corresponding Z-counterpart: Overman, L. E.; Burk, R. M. Tetrahedron Lett. 1984, 25, 5739-5742. A similar observation was noted by Fleming, see ref 7.
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27
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84987159680
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Heimstra, H.; Klaver, W. J.; Speckamp, W. N. Recl. Trav. Chim. Pays-Bas 1986, 105, 299-306.
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(1986)
Recl. Trav. Chim. Pays-Bas
, vol.105
, pp. 299-306
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Heimstra, H.1
Klaver, W.J.2
Speckamp, W.N.3
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13C NMR, IR, MS, combustion analysis, and/or HRMS AMM.
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13C NMR, IR, MS, combustion analysis, and/or HRMS AMM.
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29
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0029979532
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Similar low isolated yields (40%) have been reported in the transseries: Alvarez, E.; Delgado, M.; Diaz, M. T.; Hanxing, L.; Pérez, R.; Martin, J. D. Tetrahedron Lett. 1996, 37, 2865-2868.
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Similar low isolated yields (40%) have been reported in the transseries: Alvarez, E.; Delgado, M.; Diaz, M. T.; Hanxing, L.; Pérez, R.; Martin, J. D. Tetrahedron Lett. 1996, 37, 2865-2868.
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30
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0001206203
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Synthesis of the oxepin system: Oakes, F. T.; Yang, F.-A.; Sebastian, J. F. J. Org. Chem. 1982, 47, 3094-3097.
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Synthesis of the oxepin system: Oakes, F. T.; Yang, F.-A.; Sebastian, J. F. J. Org. Chem. 1982, 47, 3094-3097.
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0034670616
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Synthesis of the benzyl ether: Boschi, A.; Chiappe, C.; De Rubertis, A.; Ruasse, M. F. J. Org. Chem. 2000, 65, 8470-8477.
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Synthesis of the benzyl ether: Boschi, A.; Chiappe, C.; De Rubertis, A.; Ruasse, M. F. J. Org. Chem. 2000, 65, 8470-8477.
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32
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1J C-H anomeric coupling values), and finally, hydrolysis to re-yield each diastereoisomeric alcohol as a single isomer.
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1J C-H anomeric coupling values), and finally, hydrolysis to re-yield each diastereoisomeric alcohol as a single isomer.
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33
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0003536850
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Baldwin, J. E, Ed, Pergamon Press: Oxford, U.K
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Deslongchamps, P. Stereoelectronic Effects in Organic Chemistry; Baldwin, J. E., Ed.; Pergamon Press: Oxford, U.K., 1983.
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(1983)
Stereoelectronic Effects in Organic Chemistry
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Deslongchamps, P.1
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0023869410
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Synthesized from D-glucal in two steps: (a) Permethylation: Dunkerton, L. V.; Adair, N. K.; Euske, J. M.; Brady, K. T.; Robinson, P. D. J. Org. Chem. 1988, 53, 845-850.
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Synthesized from D-glucal in two steps: (a) Permethylation: Dunkerton, L. V.; Adair, N. K.; Euske, J. M.; Brady, K. T.; Robinson, P. D. J. Org. Chem. 1988, 53, 845-850.
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35
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0030824836
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Epoxidation/methanolysis: Chiappe, C.; Lo Moro, G.; Munforte, P. Tetrahedron: Asymmetry 1997, 8, 2311-2317.
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(b) Epoxidation/methanolysis: Chiappe, C.; Lo Moro, G.; Munforte, P. Tetrahedron: Asymmetry 1997, 8, 2311-2317.
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36
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The analogous perbenzylated compound has been reported ref 3b
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The analogous perbenzylated compound has been reported (ref 3b).
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37
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0029768739
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Verlhac, P.; Leteux, C.; Toupet, L.; Veyrières, A. Carbohydr. Res. 1996, 291, 11-20. Bürli, R.; Vasella, A. Helv. Chim. Acta 1996, 79, 1159-1168.
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Verlhac, P.; Leteux, C.; Toupet, L.; Veyrières, A. Carbohydr. Res. 1996, 291, 11-20. Bürli, R.; Vasella, A. Helv. Chim. Acta 1996, 79, 1159-1168.
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For example, Gin's complementary sulfonium-mediated oxidative glycosylations: Kim, J-Y.; Di Bussolo, V.; Gin, D. Y. Org. Lett. 2001, 3, 303-306.
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For example, Gin's complementary sulfonium-mediated oxidative glycosylations: Kim, J-Y.; Di Bussolo, V.; Gin, D. Y. Org. Lett. 2001, 3, 303-306.
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